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. Author manuscript; available in PMC: 2010 Feb 15.
Published in final edited form as: J Immunol. 2009 Feb 15;182(4):1892–1900. doi: 10.4049/jimmunol.0803165

Figure 1. CD8+ and NK1.1+ γδ T cell subsets undergo homeostatic expansion in TCRβ−/−δ−/− mice at distinct rates.

Figure 1

(A and B) Splenic γδ T cells were isolated from TCRβ−/− mice, labeled with CFSE, and injected into TCRβ−/−−/− recipients. Homeostatic proliferation of CD8 and CD8+ or NK1.1 and NK1.1+ γδ T cells subsets was assessed on day 5 by flow cytometry. Gates delineate those cells that have undergone at least one division, as determined by the CFSE levels of non-T cells within our donor population (unfilled grey histogram). (C) The frequency of NK1.1/CD8, NK1.1/CD8+, and NK1.1+/CD8 in the donor γδ T cell population was determined by flow cytometry. Percentages of live CD3+/TCRδ+ cells are shown for each quadrant. (D) γδ T cell reconstitution was assessed from 3 days to 2 months after transfer into TCRβ−/−−/− mice.